Department of Biotechnology, Lund University, Lund, Sweden; Department of Biology, Hacettepe University, Ankara, Turkey.
Department of Biotechnology, Lund University, Lund, Sweden; CapSenze HB, Medicon Village, SE-223 63 Lund, Sweden.
Anal Chim Acta. 2015 Sep 3;891:120-9. doi: 10.1016/j.aca.2015.07.055. Epub 2015 Aug 14.
Prostate specific antigen (PSA) is a valuable biomarker for early detection of prostate cancer, the third most common cancer in men. Ultrasensitive detection of PSA is crucial to screen the prostate cancer in an early stage and to detect the recurrence of the disease after treatment. In this report, microcontact-PSA imprinted (PSA-MIP) capacitive biosensor chip was developed for real-time, highly sensitive and selective detection of PSA. PSA-MIP electrodes were prepared in the presence of methacrylic acid (MAA) as the functional monomer and ethylene glycol dimethacrylate (EGDMA) as the cross-linker via UV polymerization. Immobilized Anti-PSA antibodies on electrodes (Anti-PSA) for capacitance measurements were also prepared to compare the detection performances of both methods. The electrodes were characterized by atomic force microscopy (AFM), scanning electron microscopy (SEM) and cyclic voltammetry (CV) and real-time PSA detection was performed with standard PSA solutions in the concentration range of 10 fg mL(-1)-100 ng mL(-1). The detection limits were found as 8.0 × 10(-5) ng mL(-1) (16 × 10(-17) M) and 6.0 × 10(-4) ng mL(-1) (12 × 10(-16) M) for PSA-MIP and Anti-PSA electrodes, respectively. Selectivity studies were performed against HSA and IgG and selectivity coefficients were calculated. PSA detection was also carried out from diluted human serum samples and finally, reproducibility of the electrodes was tested. The results are promising and show that when the sensitivity of the capacitive system is combined with the selectivity and reproducibility of the microcontact-imprinting procedure, the resulting system might be used successfully for real-time detection of various analytes even in very low concentrations.
前列腺特异性抗原(PSA)是一种用于早期检测前列腺癌(男性第三大常见癌症)的有价值的生物标志物。超敏检测 PSA 对于早期筛查前列腺癌以及检测治疗后疾病的复发至关重要。在本报告中,开发了微接触 PSA 印迹(PSA-MIP)电容式生物传感器芯片,用于实时、高灵敏度和选择性检测 PSA。通过紫外光聚合,在存在甲基丙烯酸(MAA)作为功能单体和乙二醇二甲基丙烯酸酯(EGDMA)作为交联剂的情况下制备 PSA-MIP 电极。还制备了固定在电极上的抗 PSA 抗体(Anti-PSA)用于电容测量,以比较两种方法的检测性能。通过原子力显微镜(AFM)、扫描电子显微镜(SEM)和循环伏安法(CV)对电极进行了表征,并使用浓度范围为 10 fg mL(-1)-100 ng mL(-1)的标准 PSA 溶液进行了实时 PSA 检测。检测限分别为 8.0×10(-5)ng mL(-1)(16×10(-17)M)和 6.0×10(-4)ng mL(-1)(12×10(-16)M)对于 PSA-MIP 和 Anti-PSA 电极。还针对 HSA 和 IgG 进行了选择性研究,并计算了选择性系数。还从稀释的人血清样本中进行了 PSA 检测,并最终测试了电极的重现性。结果很有希望,表明当电容系统的灵敏度与微接触印迹程序的选择性和重现性相结合时,所得系统甚至可以成功用于实时检测各种分析物,即使在非常低的浓度下也是如此。